Antianginal Drugs

34
Antianginal Drugs Antianginal Drugs Claro M. Isidro M.D.

description

 

Transcript of Antianginal Drugs

Page 1: Antianginal Drugs

Antianginal DrugsAntianginal Drugs

Claro M. Isidro M.D.

Page 2: Antianginal Drugs

Definition of termsDefinition of terms

Angina Pectoris – is the principal symptoms of patient with ischemic heart disease.

Manifested by sudden, severe, pressing substernal pain that often radiates to the left shoulder and along the flexor surface of the left arm.

Usually precipitated by exercise, excitement or a heavy meal.

Page 3: Antianginal Drugs

Types of AnginaTypes of Angina

Typical Angina ( Classical Angina ) pain is commonly induced by exercise,

excitement or a heavy meal secondary to advanced atherosclerosis of

the coronary vessels associated with ST-segment depression on

ECG

Page 4: Antianginal Drugs

Variant Angina ( Prinzmetal Angina) pain is induced while at rest associated with ST-segment elevation on

ECG secondary to vasospasm of the coronary

vesselsUnstable angina may involve coronary spasm and may also

have the component of atherosclerosis the duration of manifestation is longer than

the first two and has the manifestation of Myocardial infarction

Page 5: Antianginal Drugs

* Myocardial ischemia which produces angina results from imbalances in myocardial oxygen supply & demand relationship such as decreased oxygen supply and/or increased oxygen demand.

Etiology

1. Decrease oxygen supply

2. Increase demand for oxygen

Page 6: Antianginal Drugs

Determinant of Myocardial Oxygen Supply

1. Coronary blood flow Determined by: perfusion pressure

duration of diastole

coronary bed resistance

2. Arterio-venous oxygen difference

Page 7: Antianginal Drugs

Determinant of Myocardial Oxygen demand

Major Determinants

1. Wall stress intraventricular pressure

ventricular volume

wall thickness

2. Heart rate

3. Contractility

Page 8: Antianginal Drugs

Determinants of Vascular Tone

Relaxation of vascular smooth muscle by:

1. Increase cGMP

2. Decrease intracellular calcium

3. Increase cAMP

4. Stabilizing or preventing depolarization of the vascular smooth muscle cell membrane

Page 9: Antianginal Drugs

Treatment Plan: A. decrease the risk factor like

atherosclerosis, hypertension, smoking

B. increase oxygen supply

C. decrease oxygen demand

Page 10: Antianginal Drugs

ANTIANGINAL DRUGS

I. AGENTS WHICH ↓ O2 DEMAND & ↑ O2 SUPPLY

A. NITRATES

B. CALCIUM CHANNEL BLOCKERS

II. AGENTS WHICH ↓ O2 DEMAND

C. BETA BLOCKERS

Page 11: Antianginal Drugs

NITRATES AND NITRITESClassification of nitrates:1. Rapidly acting nitrates

* used to terminate acute attack of angina * e.g.- Nitroglycerin and Amyl nitrate * usually administered sublingually

2. Long acting nitrates * used to prevent an attack of angina * e.g. -Erythrytyl tetranitrate, Isosorbide

dinitrate, Pentaerythrytol tetranitrate * administered orally or topically

Page 12: Antianginal Drugs

NitratesNitrates

Coronary artery dilatation

Decrease coronary bed resistance (Relieved coronary vasospasm)

Increase coronary blood flow

Increase oxygen supply

Page 13: Antianginal Drugs

NitratesNitrates

Reduction on peripheral resistance(Secondary to dilatation of aorta)

Decrease blood pressure

Decrease after load

Decrease workload

Decrease oxygen consumption

Page 14: Antianginal Drugs

NitratesNitrates

Reduced venous return(Due to dilatation of the veins)

Decrease left ventricular volume

Decrease preload

Decrease workload

Decrease oxygen consumption

Page 15: Antianginal Drugs

EffectsEffects

1. Coronary artery dilatation

2. Reduction of peripheral arterial resistance – decrease after load

3. Reduce venous return – decrease preload

Page 16: Antianginal Drugs

Potential Beneficial Effects of Nitrates.

Beneficial effects Results

Decrease Ventricular vol. Decrease myocardial oxygen requirement

Decrease arterial pressure

Decrease ejection time

Venodilatation of epicardial coronary art.

Relief of coranary artery spasm

Increase collateral flow due to venodilatation

Increase perfusion to ischemic myocardium

Decrease left ventricular pressure

> decrease preload due to dilatation of the vein

> decrease after load due to dilatation of the arteries

Improved subendocardial perfusion

Page 17: Antianginal Drugs

Deleterious Effects Results

Reflex tachycardia Increase myocardial oxygen requirement

Reflex increase in contractility

Decrease diastolic perfusion

Decrease myocardial perfusion

Potential Deleterious EffectsPotential Deleterious Effects

Page 18: Antianginal Drugs

ROUTES OF ADMINISTRATION

1. Sublingual route – rational and effective for the treatment of acute attacks of angina pectoris. Half-life depend only on the rate at which they are delivered to the liver.2. Oral route – to provide convenient and prolonged prophylaxis against attacks of angina3. Intravenous Route – useful in the treatment of coronary vasospasm and acute ischemic syndrome.4. Topical route – used to provide gradual absorption of the drug for prolonged prophylactic purpose.

Page 19: Antianginal Drugs

Drug Usual single dose Route of administration

Duration of action

Short acting

Nitroglycerin

0.15-1.2 mg sublingual 10 - 30 min

Isosorbide dinitrate 2.5-5 mg sublingual 10 – 60 min

Amyl nitrite 0.18 – 3 ml inhalation 3 – 5 min

Long acting

Nitroglycerin sustained action

6.5 – 13 mg q 6-8 hrs oral 6 – 8 hrs

Nitroglycerin 2% ointment

1 – 1.5 inches q hr topical 3 – 6 hrs

Niroglycerin slow released

1 –2 mg per 4 hrs Buccal mucosa 3 – 6 hrs

Nitroglycerin slow released

10 – 25 mg /24hrs (one patch/day}

transdermal 8 –10 hrs

Isosorbide dinitrate 2.5 – 10 mg per 2 hrs sublingual 1.5 – 2 hrs

Isosorbide dinitrate 10 –60 mg per 4-6 hrs oral 4 – 6 hrs

Isosorbide dinitrate chewable

5 – 10 mg per 2-4 hrs oral 2 – 3 hrs

Isosorbide mononitrate 20 mg per 12 hrs oral 6 –10 hrs

Page 20: Antianginal Drugs

Adverse EffectsAdverse Effects

1. Throbbing headache

2. Flushing of the face

3. Dizziness – especially at the beginning of treatment

4. Postural Hypotension – due to pooling of blood in the dependent portion of the body

Page 21: Antianginal Drugs

ContraindicationContraindication

1. Renal ischemia

2. Acute myocardial infarction

3. Patients receiving other antihypertensive agent

Page 22: Antianginal Drugs

B-BlockersB-Blockers

Hemodynamics Effects

1.  Decrease heart rate

2. Reduced blood pressure and cardiac contractility without appreciable decrease in cardiac output

Page 23: Antianginal Drugs

B-BlockersB-Blockers

Decrease heart rate & Contractility

Increase duration of diastole

Decrease workload

Increase coronary blood flow

Decrease O2 consumption

Increase oxygen supply

Page 24: Antianginal Drugs

ContraindicationContraindication

1. Congestive heart failure

2. Asthma

3. Complete heart block

Page 25: Antianginal Drugs

Ca - Channel BlockersCa - Channel Blockers

Effects1. Coronary artery dilatation

2. Reduction on peripheral arterial resistance – decrease after load

Page 26: Antianginal Drugs

Ca Channel BlockersCa Channel Blockers

Coronary artery dilatation

Decrease coronary bed resistance (Relieved coronary vasospasm)

Increase coronary blood flow

Increase oxygen supply

Page 27: Antianginal Drugs

Ca channel BlockersCa channel Blockers

Reduction on peripheral resistance

(Secondary to dilatation of aorta)

Decrease blood pressure

Decrease after load

Decrease workload

Decrease oxygen consumption

Page 28: Antianginal Drugs

Most commonly used Ca Channel Blockers1. Nifedipine2. Verafamil3. Diltiazem

Pharmacokineticss

Drugs Onset of action Peak of action Half-life

Nifedipine 20 minutes 1 hour 3-4 hours

Verafamil 1-2 hours 5 hours 8-10 hours

Diltiazem 15 minutes 30 minutes 3-4 hours

Nicardifine 20 minutes 45 minutes 2-4 hours

Felodipine 2-5 hours 6-7 hours 11-16 hour

Page 29: Antianginal Drugs

Unwanted effect Nausea and vomiting Dizzyness Flushing of the face Tachycardia – due to hypotension

Contraindications Cardiogenic shock Recent myocardial infarction Heart failure Atrio-ventricular block

Page 30: Antianginal Drugs

Combination Theraphy1. Nitrates and B-blockers * The additive efficacy is primarily a

result of one drug blocking the adverse effect of the other agent on net myocardial oxygen consumption

* B-blockers – blocks the reflex tachycardia associated with nitrates

* Nitrates – attenuate the increase in the left ventricular end diastolic volume associated with B-lockers by increasing venous capacitance

Page 31: Antianginal Drugs

2. Ca channel blockers and B-blockers * useful in the treatment of exertional

angina that is not controlled adequately with nitrates and B-blockers

* B-blockers – attenuate reflex tachycardia produce by nifedipine

* These two drugs produce decrease blood pressure

Page 32: Antianginal Drugs

3. Ca channel blockers and Nitrates * Useful in severe vasospastic or

exertional angina (particularly in patient with exertional angina with congestive heart failure and sick sinus syndrome)

* Nitrates reduce preload and after load

* Ca channels reduces the after load

* Net effect is on reduction of oxygen demand

Page 33: Antianginal Drugs

4. Triple drugs – Nitrate + Ca channel blockers + B-blockers

*Useful in patients with exertional angina not controlled by the administration of two types of anti-anginal agent

* Nifidipine – decrease after load

Nitrates – decrease preload

B-blockers – decrease heart rate & myocardial contractility

Page 34: Antianginal Drugs

Type of Angina

Other Names Description Drug Therapy

STABLE Classic

Exertional

Fixed

Atherosclerotic

Obstruction coronary artery

Nitrates

CCB

B-blockers

VARIANT Prinzmetal’s

Vasospasmic

Vasospasm at any time

Nitrates

CCB

UNSTABLE Crescendo Combined effect

Pre= MI

Nitrates

CCB